Predictive Characteristics of Malignant Pheochromocytoma

Pheochromocytoma is a catecholamine-secreting tumor that emerges from the chromaffin cells of the adrenal medulla, usually manifesting as a benign tumor but occasionally becoming malignant [1, 2]. Because the long-term prognosis of patients with malignant pheochromocytoma is unclear or poor, identification of factors associated with malignancy could aid in modifying follow-up plans and could enhance disease-specific survival. Previous studies on malignant pheochromocytoma have mostly been anecdotal, and efforts to clinically, biochemically, and radiographically distinguish between benign and malignant pheochromocytoma have been inconsistent [3, 4]. Partly, these may have been because of the low incidence of the tumor and the limited postoperative follow-up with inconsistent protocols. Therefore, from a single institutional database, we aimed to identify potential clinical characteristics predictive of differentiating malignant pheochromocytomas from benign pheochromocytomas.

Our study consisted of 152 patients treated surgically between 1989 and 2008 at our hospital. The 152 patients consisted of 81 men and 71 women, aged 18 to 76 years (median, 46.5 years). Of these, 135 had benign tumors and 17 had malignant tumors (5 at the initial diagnosis and 12 subsequently diagnosed during follow-up). The clinical diagnosis of malignancy in the 17 patients was based on the presence of metastatic lesions either at diagnosis or during follow-up.

Preoperatively, tumors were localized by computed tomography (CT) and/or magnetic resonance imaging (MRI). Also, metaiodobenzylguanidine-131 (MIBG) scans were performed in patients with suspected extra-adrenal or malignant pheochromocytoma. Twenty-four-hour urinary concentrations of vanillylmandelic acid (VMA), epinephrine, norepinephrine, metanephrine, and dopamine were assessed in most patients. Postoperative follow-up included blood pressure measurement, CT, and MIBG scan every 6 months for 2 years and annually thereafter in the absence of recurrence. Urinary catecholamines were followed when elevated levels were observed at 6 months postoperatively. Patients were followed for a mean of 41.5 months (range, 0.9-298 months) after surgery.

Factors compared between the two groups included clinical (age, gender, symptoms, interval to diagnosis from symptom onset, associated syndromes, postoperative hypertension), radiographical (tumor location, tumor size), and biochemical (urinary catecholamine levels) variables. The 24-hour urinary catecholamine levels per unit diameter of tumor were calculated to account for the differences in tumor size.

For statistical analyses, we used the chi-squared test and the Mann-Whitney U test for comparison between the benign and the malignant characteristics. Cutoff values for tumor size and VMA per unit of tumor diameter were calculated by receiver operating characteristic (ROC) analysis for predicting the 5-year metastasis-free survival rate. Survival curves were determined by using the Kaplan-Meier method and were compared by the log-rank test. For all analyses, SPSS ver. 12.0 (SPSS Inc., Chicago, IL, USA) was used, and a p-value<0.05 was set for significance.

There were 17 patients with metastatic pheochromocytomas. Initially metastatic lesions (n=5) were found in the lung (2), liver (1), bone (1), and distant lymph node (1). Metachronous metastases occurred on average 49.4 months (range, 5.9-194.8 months) postoperatively. The locations of recurrent disease were liver (6), bone (4), lung and pleura (4), and bladder (1). Patients were diagnosed with pheochromocytoma, either benign or malignant, within 0.02 months to 7.2 years (median, 1.8 years) from the onset of symptoms. Familial syndromes, including von Hippel-Lindau syndrome, were present in three patients with benign tumors but in none of those with malignancies. Of the 152 tumors, 137 (90.1%) were adrenal, 14 (9.2%) were solitary extra-adrenal, and 1 (0.7%) was multiple extra-adrenal. In particular, 11 (8%) of the 135 benign tumors were extra-adrenal, compared with 4 (24%) of the 17 malignant tumors. The single multiple extra-adrenal tumor was malignant, whereas the seven bilateral adrenal tumors were benign. Of the extra-adrenal pheochromocytomas, two malignant and five benign tumors were located in the periaortic (Zuckerkandl) bodies, and the remainder were in the retroperitoneum, bladder, and other organs (Table 1).

TABLE 1
Comparison of clinical characteristics of patients with benign and malignant pheochromocytomas

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Malignant tumors were significantly larger than benign pheochromocytomas (11.1±4.0 vs. 6.2±3.4 cm, p<0.001) (Table 1). However, age and gender showed no significant correlations with malignancy. In addition, the most frequent symptoms in patients with both benign and malignant pheochromocytomas were headache, palpitations, and excessive sweating, without differences between the groups. Whereas blood pressure generally became normal after adrenalectomy, arterial hypertension persisted after removal more frequently in malignant tumors (23.5% vs. 0.7%, p=0.001).

Preoperatively, total 24-hour urinary excretion of the catecholamines VMA, epinephrine, norepinephrine, metanephrine, and dopamine was significantly enhanced in patients with both malignant and benign pheochromocytomas, without differences between the groups (Table 1). However, when the urinary catecholamines excreted per unit of tumor were compared, patients with malignant tumors excreted significantly lower amounts of epinephrine (4.0 vs. 168.9 µg/day/cm, p=0.010) than did patients with benign tumors (Fig. 1A). Furthermore, among the 147 patients without metastatic disease at the initial diagnosis, those who later developed metastasis also had significantly reduced 24-hour urinary excretion of the catecholamine metabolites VMA (1.2 vs. 3.7 mg/day/cm, p=0.049), epinephrine (4.5 vs. 168.9 µg/day/cm, p=0.008), and norepinephrine (13.1 vs. 121.8 mg/day/cm, p<0.001) than did those with benign tumors (Fig. 1B).

FIG. 1
Comparison of 24-hour urinary catecholamine secretion in patients with benign and malignant pheochromocytomas (A: benign vs. all cases malignant, B: benign vs. postoperative recurrent malignant).

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The overall 5-year metastasis-free survival rate was 84.4%. The areas under the ROC curves for predicting the 5-year metastasis-free survival rate were 0.783 (95% CI: 0.652-0.914) for tumor size and 0.767 (95% CI: 0.674-0.920) for VMA per unit of tumor diameter. The tumor size cutoff for prediction of survival rates was calculated to be 5.5 cm (sensitivity 86.7%, specificity 56.7%), and the VMA per unit of tumor diameter cutoff value was calculated to be 2.1 mg/day/cm (sensitivity 85.5%, specificity 58.1%). Survival rates were significantly higher in patients with smaller tumors (≤5.5 cm vs. >5.5 cm; 90.6 vs. 81.2%, p=0.025) and in those with higher 24-hour urinary VMA per unit of tumor diameter (>2.1 vs. ≤2.1 mg/day/cm; 94.9 vs. 70.9%, p=0.019) (Fig. 2). The 5-year survival rate of patients with malignant pheochromocytoma was 11.8%. Among patients with malignant disease, 1 patient received palliative radiotherapy and 5 received palliative MIBG therapy, resulting in modulation of the symptoms of catecholamine hyperproduction. Although six patients received palliative combined chemotherapy (cyclophosphamide/adriamycin), none demonstrated response to any chemotherapeutic agents and all progressed.

FIG. 2
Metastasis-free survival relative to tumor size (A) and 24-hour urinary secretion of VMA/unit of tumor diameter (B).

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Clinical behavior, including invasion of adjacent tissues and the presence of metastases at non-chromaffin sites, is the only currently accepted indication of malignant pheochromocytoma [5, 6]. We found that the incidence of malignant pheochromocytomas among 152 patients with pheochromocytomas was 11.2%, in good agreement with the 8% to 12.5% previously reported [7-11]. We also found that the 5-year survival rate of our patients with malignant pheochromocytoma was 11.8%, which was thus somewhat lower than the 20% previously reported [12]. Although none of our patients with malignant pheochromocytomas were alive after 10 years, others have reported somewhat better results [2]. The poor prognosis of patients with malignancy is thought to be attributable to dissemination to other organs, along with the heart failure associated with hypercatecholaminemia [6, 13-18]. Thus, long-term prognosis will not improve unless other features that can predict malignant behavior can be identified.

Previous studies have not been successful in identifying distinctive factors for malignant pheochromocytoma. Although some histopathological features have been suggested to be associated with an increased incidence of malignancy, including tumor necrosis, mitosis rate >3/30 HPF, capsular invasion, vascular invasion, large nests with central degeneration, a lack of hyaline globules, a high nuclear/cytoplasmic ratio, monotony of cytological pattern, and spindle cell patterns [6, 17, 19], none of these differences is sufficiently diagnostic. Moreover, molecular markers, including telomerase [20], inhibins, activins [21], endothelial Per-ARNT-Sim domain protein-1, vascular endothelial growth factor, endothelin receptor type B [22], and cyclooxygenase [21], have been found to be significant but unreliable and not readily applicable for distinguishing benign from malignant pheochromocytomas. Moreover, in assaying clinical parameters, we found that age, gender, symptoms, and delay in diagnosis did not correlate with the presence of either benign or malignant pheochromocytoma. Although extra-adrenal tumor location was associated with malignancy to some extent, the relationship was not significant (p=0.068).

We found, however, that malignant tumors were significantly larger than were benign tumors at presentation (11.1±4.0 vs. 6.2±3.4 cm, p<0.001). Although similar results have been reported (median tumor size, 8 cm vs. 5.1 cm, respectively), no cutoff values for size and weight were found to differentiate benign from malignant tumors [23]. In contrast, we found that the use of a size cutoff of 5.5 cm could distinguish 5-year metastasis-free survival rates in patients with benign and malignant tumors (90.6% vs. 81.2%, p=0.025). In contrast with studies reporting that malignant tumors secrete more metanephrines than do benign tumors [19, 24, 25], we found that the 24-hour urinary excretion per tumor diameter unit of the catecholamine metabolites VMA and epinephrine was significantly lower in patients with malignant tumors than in those with benign tumors, whereas the total excretions were similar. In particular, patients without metastatic disease at diagnosis showed more distinct differences in the secretion of the urinary catecholamine metabolites VMA, epinephrine, norepinephrine, and metanephrine. Necrosis in the tumor center, especially in large tumors, has been suggested to account for lower secretion in hormone-producing tumors [26]. However, in our study, gross tumor necrosis was observed in only 5 of the patients and our results demonstrate that the catecholamines produced per unit of tumor instead of the total mass were significantly lower. We speculate that tumors cells with malignant potential may intrinsically carry less functional capacity because of under-differentiation.

In agreement with earlier studies, which showed that persistent postoperative arterial hypertension was more common in patients with malignant than benign pheochromocytomas, we found that arterial hypertension persisted after tumor removal in 1 of 135 (0.7%) patients with benign tumors and in 4 of 17 (23.5%) with malignant pheochromocytomas, likely due to occult metastasis. Monitoring arterial blood pressure after successful surgery may provide a clue for potential development of subsequent metastasis. Postoperative metastasis or recurrence was observed within 4.2 years of surgical treatment in 9 of 12 patients (75%) with malignancy, with a median time from primary excision to metastasis of 16.8 months (range, 4.8-194.8 months). These findings suggest that patients at risk should undergo more rigorous follow-up with the use of imaging modalities such as postoperative CT and MIBG scanning for at least 2 years and with the use of biochemical modalities such as low 24-hour urinary catecholamine excretion within 4 months after surgery.

The retrospective design of our study and the relatively small number of patients from a single institution limit the interpretation of our study results. Furthermore, in the urinary catecholamine analysis, although we noted a higher significance with epinephrine and norepinephrine, we suggested a cutoff for VMA because it is the most widely and specifically used index for diagnosing pheochromocytoma, and data were not available for some of the other indexes. Thus, the predictive characteristics identified here require confirmation in a larger, prospective, multicenter study. In particular, further research on the long-term prognostic value of pre- and postoperative 24-hour urinary catecholamine excretion would seem worthwhile.

In patients with pheochromocytoma, large tumor size (>5.5 cm) and minimally elevated 24-hour urinary VMA (≤2.1 mg/day/cm) were significantly associated with a higher probability of the tumor being a malignancy, thus portending a lower metastasis-free survival. Thus, patients with these characteristics mandate more rigorous follow-up after surgery.